Our mission is to provide a comprehensive and compassionate online resource for individuals living with lupus, their families, and the broader community. Through our blog, we aim to empower and educate readers about lupus, its symptoms, treatments, and lifestyle management strategies. Our commitment is to foster a supportive and inclusive space where individuals can find knowledge, inspiration, and connection. By sharing personal stories, expert insights, and the latest research, we strive to raise awareness about lupus, reduce stigma, and promote a better understanding of this complex autoimmune condition. Together, we will navigate the challenges of lupus, advocate for improved care, and provide a sense of solidarity for the lupus community worldwide.
Lupus mean “wolf ” in latin
My name is Teika I was diagnoise with lupus at the age of 19. I went into acoma and died for 3 minutes obiously I don’t rember andy of this. I had gotten spinal miningitis from a classmate. After over 60 days in the hospital I was told I had lupus. My sister had M.S and my sister in law has lupus so I had a good idea of what my life would be like from that day on.
